中文

Journal Publications

[21]谭跃球, Tu C, Meng L, Nie H, Yuan S, Wang W, Du J, Lu G, Lin G, Tan YQ*. A homozygous RPL10L missense mutation associated with male factor infertility and severe oligozoospermia[J].Fertil Steril, 2020, 113 (3) : 561-568.
[22]Zhang YX, He WB, Xiao WJ, Meng LL, Tan C, Du J, Lu GX, Lin G, Tan YQ*. Novel loss-of-function mutation in MCM8 causes premature ovarian insufficiency.Mol Genet Genomic Med, 2020, 8 (4) : e1165.
[23]谭跃球, Tu C, Nie H, Meng L, Wang W, Li H, Yuan S, Cheng D, He W, Liu G, Du J, Gong F, Lu G, Lin G.Tu C, Nie H, Meng L, Wang W, Li H, Yuan S, Cheng D, He W, Liu G, Du J, Gong F, Lu G, Lin G, Zhang Q, Tan YQ*. Novel mutations in SPEF2 causing different defects between flagella and cilia bridge: the phenotypic link between MMAF and PCD[J].Hum Genet, 2020, 139 (2) : 257-271.
[24]Tan YQ*, Lin G, Lu G, Lu C, Gong F, Xu F, Luo K, Yi D, Yuan S, Cheng D.Cheng D, Yuan S, Yi D, Luo K, Xu F, Gong F, Lu C, Lu G, Lin G, Tan YQ*. Analysis of molecular cytogenetic features and PGT-SR for two infertile patients with small supernumerary marker chromosomes[J].J Assist Reprod Genet, 2019, 11 (12) : 2533-2539.
[25]Tan YQ*, Lin G, Lu G, Du J, Li W, Li H, Luo A, He W, Yuan S, Meng L, Nie H, Tu C.Tu C, Nie H, Meng L, Yuan S, He W, Luo A, Li H, Li W, Du J, Lu G, Lin G, Tan YQ*. Identification of DNAH6 mutations in infertile men with multiple morphological abnormalities of the sperm flagella[J].Sci Rep, 2019, 9 (1) : 15864.
[26]Tan Y*, Lin G, Lu GX, Fan L, Gong F, Wang J, Du J, Zhang Q, Li Y, Meng L, Nie H, Tu C, Wang W.Wang W, Tu C, Nie H, Meng L, Li Y, Yuan S, Zhang Q, Du J, Wang J, Gong F, Fan L, Lu GX, Lin G, Tan YQ*. Biallelic mutations in CFAP65 lead to severe asthenoteratospermia due to acrosome hypoplasia and flagellum malformations[J].J Med Genet, 2019, 56 (11) : 750-757.
[27]Xiao WJ, He WB, Zhang YX, Meng LL, Lu GX, Lin G, Tan YQ*, Du J*. In-Frame variants in STAG3 gene cause premature ovarian insufficiency[J].Front Genet., 2019, 10: 1016.
[28]Tan YQ*, Li W, Lin G, Lu GX, Zhang YX, Zhou S, Xie PY, Du J, He WB.He WB, Du J, Xie PY, Zhou S, Zhang YX, Lu GX, Lin G, Li W, Tan YQ*. X-chromosome inactivation pattern of amniocytes predicts the risk of dystrophinopathy in fetal carriers of DMD mutations[J].Prenat Diagn, 2019, 39 (8) : 603-608.
[29]Lin G, Lu GX, Zhong CG, Gong F, Li W, Du J, Luo AX, Sjaarda C, Yuan SM, Meng LL, Tu CF, Tan YQ*.Tan YQ, Tu CF, Meng LL, Yuan SM, Sjaarda C, Luo AX, Du J, Li W, Gong F, Zhong CG, Deng HX, Lu GX, Liang P, Lin G. Loss-of-function mutations TDRD7 lead to a rare novel syndrome combining congenital cataract and non-obstructive azoospermia in humans[J].Genetics in Medicine, 2019, 21 (5) : 1209-1217.
[30]Tan YQ*, Yang Y, Lin G, Lu GX, Li W, Du J, Tu C, He WB, Li HY, Zhang YX.Zhang YX, Li HY, He WB, Tu C, Du J, Li W, Lu GX, Lin G, Yang Y, Tan YQ*. XRCC2 mutation causes premature ovarian insufficiency as well as non-obstructive azoospermia in humans[J].Clin Genet, 2019, 95 (3) : 442-443.
[31]Tan YQ*, Lu GX, Lin G, Tu CF, Yuan SM, Meng LL.Meng LL, Yuan SM, Tu CF, Lin G, Lu GX, Tan YQ*. Next-generation sequencing identified a novel SPTB frameshift insertion causing hereditary spherocytosis in China[J].Ann Hematol, 2019, 98 (1) : 223-226.
[32]？Tan Y*, Lin G, Lu G, Tu C, Meng L.Meng L, Tu C, Lu G, Lin G, Tan Y*. Novel biallelic PCNT deletion causing microcephalic osteodysplastic primordial dwarfism type II with congenital heart defect[J].Sci China Life Sci, 2019, 62 (1) : 144-147.
[33]Tan YQ*, Liu Q.Liu Q, Tan YQ*. Advances in Identifications of Susceptibility Gene Defects of Hereditary Colorectal Cancer[J].J Cancer, 2019, 10 (3) : 643-653.
[34]Tan YQ*, Lu GX, ？Lin G, Meng LL, Tu CF, Li W, Du J, Zhang YN, Yuan SM.Yuan SM, Zhang YN, Du J, Li W, Tu CF, Meng LL, Lin G, Lu GX, Tan YQ*. Phenotypic and molecular characteristics of androgen insensitivity syndrome patients[J].Asian J Androl, 2018, 20 (5) : 473-478.
[35]Tan YQ*, Zhang W, ？Lin G, Yang C, Zhang Y, Du J, Li H, Yuan S, Cheng D, Luo A.Luo A, Cheng D, Yuan S, Li H, Du J, Zhang Y, Yang C, Lin G, Zhang W, Tan YQ*. Maternal interchromosomal insertional translocation leading to 1q43-q44 deletion and duplication in two siblings[J].Mol Cytogenet, 2018, 11: 24.
[36]Tan YQ*, Lu GX, Lin G, Xu DB, Du J, Tu CF, Huang H, Yuan SM.Yuan SM, Huang H, Tu CF, Du J, Xu DB, Lin G, Lu GX, Tan YQ*. A rare polypyrimidine tract mutation in the androgen receptor gene results in complete androgen insensitivity syndrome[J].Asian J Androl, 2018, 20 (3) : 308-310.
[37]Tan YQ*, Lin G, Lu GX, Zhong CG, Du J, Li W, Shen J, He FS, Yuan SM, Meng LL, Liu Q, Tu CF, He WB.He WB, Tu CF, Liu Q, Meng LL, Yuan SM, Luo AX, He FS, Shen J, Li W, Du J, Zhong CG, Lu GX, Lin G, Fan LQ, Tan YQ*. DMC1 mutation that causes human non-obstructive azoospermia and premature ovarian insufficiency identified by whole-exome sequencing[J].J Med Genet, 2018, 55 (3) : 198-204.
[38]Tan YQ*, Gong F, Lin G, Lu GX, Zhang YX, Chen YZ, Dai C, Tang WL, Li W, Yang XW, Du J, He WB.He WB, Du J, Yang XW, Li W, Tang WL, Dai C, Chen YZ, Zhang YX, Lu GX, Lin G, Gong F, Tan YQ*. Novel inactivating mutations in the FSH receptor cause premature ovarian insufficiency with resistant ovary syndrome[J].Reprod Biomed Online, 2018, 38 (3) : 397-406.
[39]Tan YQ*, Du J, Lin G, Lu GX, Zhong CG, Li XR, Li W, Gong F, He WB, Yang XW.Yang XW, He WB, Gong F, Li W, Li XR, Zhong CG, Lu GX, Lin G, Du J, Tan YQ*. Novel FOXL2 mutations cause blepharophimosis-ptosis-epicanthus inversus syndrome with premature ovarian insufficiency[J].Mol Genet Genomic Med, 2018, 6 (2) : 261-267.
[40]Tan YQ*, Lu G, Lin G, Luo A, Meng L, Tu C, Yuan S, Xiong B, Yi D, He W, Cheng D, Li W, Du J, Li H.Li H, Du J, Li W, Cheng D, He W, Yi D, Xiong B, Yuan S, Tu C, Meng L, Luo A, Lin G, Lu G, Tan YQ*. Rare partial octosomy and hexasomy of 15q11-q13 associated with intellectual impairment and development delay: report of two cases and review of literature[J].Mol Cytogenet, 2018, 11: 15.

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